Variant report

Variant	nsv518097
Chromosome Location	chr15:58959273-58964931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58961444-58961957	K562	blood:	n/a	chr15:58961720-58961736
2	ATF1	chr15:58961450-58961769	K562	blood:	n/a	n/a
3	CCNT2	chr15:58961404-58961791	K562	blood:	n/a	chr15:58961565-58961585
4	CEBPD	chr15:58961329-58961797	K562	blood:	n/a	n/a
5	CUX1	chr15:58961361-58961731	K562	blood:	n/a	n/a
6	EP300	chr15:58961376-58961768	K562	blood:	n/a	n/a
7	FOS	chr15:58959172-58959530	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
8	FOS	chr15:58959175-58959509	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
9	FOS	chr15:58959172-58959509	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
10	FOS	chr15:58959163-58959498	MCF10A-Er-Src	breast:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
11	FOSL2	chr15:58959039-58959640	A549	lung:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
12	GATA2	chr15:58961344-58961803	K562	blood:	n/a	chr15:58961575-58961583
13	IRF1	chr15:58961477-58962011	K562	blood:	n/a	n/a
14	JUN	chr15:58959169-58959450	HUVEC	blood vessel:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959340-58959351 chr15:58959345-58959352
15	JUND	chr15:58959256-58959400	HepG2	liver:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959342-58959353 chr15:58959340-58959351 chr15:58959345-58959352
16	JUND	chr15:58959195-58959546	H1-hESC	embryonic stem cell:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959342-58959353 chr15:58959340-58959351 chr15:58959345-58959352
17	JUND	chr15:58961406-58961767	K562	blood:	n/a	n/a
18	JUND	chr15:58959162-58959520	Hela-S3	cervix:	n/a	chr15:58959343-58959353 chr15:58959344-58959352 chr15:58959342-58959353 chr15:58959340-58959351 chr15:58959345-58959352
19	MAFK	chr15:58959616-58959659	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr15:58961407-58961740	K562	blood:	n/a	n/a
21	NR2F2	chr15:58961373-58961759	K562	blood:	n/a	chr15:58961526-58961541
22	POLR2A	chr15:58959423-58959596	K562	blood:	n/a	n/a
23	POLR2A	chr15:58964523-58964552	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr15:58959254-58959688	HepG2	liver:	n/a	n/a
25	POLR2A	chr15:58960614-58960654	Hela-S3	cervix:	n/a	n/a
26	RAD21	chr15:58959160-58959529	IMR90	lung:	n/a	n/a
27	RCOR1	chr15:58961426-58961779	K562	blood:	n/a	n/a
28	SMC3	chr15:58959994-58960049	GM12878	blood:	n/a	n/a
29	STAT3	chr15:58959387-58959587	MCF10A-Er-Src	breast:	n/a	n/a
30	TAL1	chr15:58961377-58961802	K562	blood:	n/a	chr15:58961503-58961514 chr15:58961565-58961583 chr15:58961500-58961515 chr15:58961500-58961515 chr15:58961501-58961512
31	TCF12	chr15:58959062-58959753	A549	lung:	n/a	n/a
32	TEAD4	chr15:58961368-58961753	K562	blood:	n/a	n/a
33	TEAD4	chr15:58961338-58961822	K562	blood:	n/a	n/a
34	USF1	chr15:58961368-58961667	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58960059-58960109	NB4	blood:	n/a
2	chr15:58960059-58960109	U87	brain:	n/a
3	chr15:58960059-58960109	HL-60	blood:	n/a
4	chr15:58960059-58960109	CMK	blood:	n/a
5	chr15:58960059-58960109	HAEpiC	amniotic membrane:	n/a
6	chr15:58960059-58960109	Hepatocyte	liver:	n/a
7	chr15:58960059-58960109	HCT-116	colon:	n/a
8	chr15:58960059-58960109	AG09319	gingival:	n/a
9	chr15:58960059-58960109	AG09309	skin:	n/a
10	chr15:58960059-58960109	T-47D	breast:	n/a
11	chr15:58960059-58960109	PrEC	prostate:	n/a
12	chr15:58960059-58960109	MCF10A-Er-Src	breast:	n/a
13	chr15:58960059-58960109	AG04449	skin:	fetal
14	chr15:58960059-58960109	HepG2	liver:	n/a
15	chr15:58960059-58960109	ProgFib	skin:	n/a
16	chr15:58960059-58960109	PANC-1	pancreas:	n/a
17	chr15:58960059-58960109	ECC-1	luminal epithelium:	n/a
18	chr15:58960059-58960109	K562	blood:	n/a
19	chr15:58960059-58960109	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:58960059-58960109	HMEC	breast:	n/a
21	chr15:58960059-58960109	GM12891	blood:	n/a
22	chr15:58960059-58960109	ovcar-3	ovarian:	n/a
23	chr15:58960059-58960109	HCF	heart:	n/a
24	chr15:58960059-58960109	AoSMC	blood vessel:	n/a
25	chr15:58960059-58960109	A549	lung:	n/a
26	chr15:58960059-58960109	LNCaP	prostate:	n/a
27	chr15:58960059-58960109	BJ	skin:	n/a
28	chr15:58960059-58960109	GM06990	blood:	n/a
29	chr15:58960059-58960109	HUVEC	blood vessel:	n/a
30	chr15:58960059-58960109	AG10803	skin:	n/a
31	chr15:58960059-58960109	HEEpiC	esophagus:	n/a
32	chr15:58960059-58960109	Jurkat	blood:	n/a
33	chr15:58960059-58960109	GM12892	blood:	n/a
34	chr15:58960059-58960109	NH-A	brain:	n/a
35	chr15:58960059-58960109	HRE	kidney:	n/a
36	chr15:58960059-58960109	Caco-2	colon:	n/a
37	chr15:58960059-58960109	HRCEpiC	kidney:	n/a
38	chr15:58960059-58960109	H1-hESC	embryonic stem cell:	embryo
39	chr15:58960059-58960109	HRPEpiC	eye:	n/a
40	chr15:58960059-58960109	HNPCEpiC	eye:	n/a
41	chr15:58960059-58960109	SK-N-SH_RA	brain:	n/a
42	chr15:58960059-58960109	SAEC	small airway:	n/a
43	chr15:58960059-58960109	GM12878	blood:	n/a
44	chr15:58960059-58960109	NHDF-neo	bronchial:	n/a
45	chr15:58960059-58960109	HIPEpiC	eye:	n/a
46	chr15:58960059-58960109	HCPEpiC	choroid plexus:	n/a
47	chr15:58960059-58960109	HEK293	kidney:	embryo
48	chr15:58960059-58960109	IMR90	lung:	fetal
49	chr15:58960059-58960109	RPTEC	kidney:	n/a
50	chr15:58960059-58960109	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58959008..58961763-chr15:58963675..58966633,2	K562	blood:
2	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
3	chr15:58957306..58961861-chr15:58967060..58970416,4	K562	blood:
4	chr15:58950082..58952311-chr15:58956735..58959470,2	K562	blood:
5	chr15:58953177..58955880-chr15:58958454..58961862,3	K562	blood:
6	chr15:58949134..58952311-chr15:58956735..58961509,4	K562	blood:
7	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
8	chr15:58956671..58958559-chr15:58959977..58961761,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM63B-5	chr15:58964495-58965132	NONHSAT044121

Variant related genes	Relation type
ENSG00000270986	TF binding region
ENSG00000270986	CpG island
ENSG00000270986	chromatin interactions

Extended variants
information (count: 211 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:211 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1427281	chr15:58959273-58959274	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532444793	chr15:58959325-58959326	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546060904	chr15:58959344-58959345	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559575080	chr15:58959354-58959355	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560131552	chr15:58959374-58959375	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34665053	chr15:58959409-58959410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548290125	chr15:58959471-58959472	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577853681	chr15:58959488-58959489	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7177678	chr15:58959621-58959622	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542681251	chr15:58959631-58959632	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530529685	chr15:58959693-58959694	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550301805	chr15:58959719-58959720	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570051301	chr15:58959757-58959758	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538927308	chr15:58959791-58959792	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572198395	chr15:58959813-58959814	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552382074	chr15:58959869-58959870	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368762505	chr15:58959890-58959891	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368867363	chr15:58959936-58959937	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113725859	chr15:58959959-58959960	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs75137596	chr15:58959970-58959971	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565954793	chr15:58959977-58959978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534870704	chr15:58959993-58959994	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs143042590	chr15:58960038-58960039	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373372444	chr15:58960043-58960044	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574793852	chr15:58960044-58960045	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537500547	chr15:58960060-58960061	Enhancers Weak transcription Strong transcription	CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145296485	chr15:58960062-58960063	Enhancers Weak transcription Strong transcription	CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs377036517	chr15:58960123-58960124	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573866552	chr15:58960154-58960155	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542513569	chr15:58960220-58960221	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577244966	chr15:58960288-58960289	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs137880186	chr15:58960307-58960308	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141608651	chr15:58960378-58960379	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377512241	chr15:58960426-58960427	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562801698	chr15:58960445-58960446	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541622002	chr15:58960508-58960509	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150537567	chr15:58960534-58960535	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530510082	chr15:58960687-58960688	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183309029	chr15:58960697-58960698	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531371527	chr15:58960712-58960713	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563715976	chr15:58960727-58960728	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370408823	chr15:58960729-58960730	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs532738705	chr15:58960756-58960757	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35581767	chr15:58960818-58960819	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188142844	chr15:58960837-58960838	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561271756	chr15:58960838-58960839	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565991617	chr15:58960866-58960867	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139501517	chr15:58960896-58960897	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548494804	chr15:58960932-58960933	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149302192	chr15:58960937-58960938	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58891400-58959600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr15:58905000-58983200	Weak transcription	Esophagus	oesophagus
3	chr15:58905400-58971800	Weak transcription	Spleen	Spleen
4	chr15:58905600-58976400	Weak transcription	Gastric	stomach
5	chr15:58906400-58976400	Weak transcription	Small Intestine	intestine
6	chr15:58917000-58959600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:58921200-58959600	Weak transcription	Aorta	Aorta
8	chr15:58921200-58968400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr15:58921600-58976600	Weak transcription	Right Ventricle	heart
10	chr15:58921800-58970400	Weak transcription	Stomach Mucosa	stomach
11	chr15:58923400-58971800	Weak transcription	Pancreas	Pancrea
12	chr15:58923400-58982800	Weak transcription	Lung	lung
13	chr15:58924000-58960000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr15:58933000-58987000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr15:58934200-58976400	Weak transcription	Psoas Muscle	Psoas
16	chr15:58936000-58977000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr15:58936200-58991400	Weak transcription	HMEC	breast
18	chr15:58945600-58959400	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr15:58947200-58959600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr15:58947800-58971800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:58947800-58976400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr15:58948000-58959400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr15:58949400-58976400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr15:58951000-58959600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr15:58951200-58987000	Weak transcription	NHEK	skin
26	chr15:58951400-58959400	Strong transcription	Fetal Thymus	thymus
27	chr15:58951600-58961400	Weak transcription	Fetal Lung	lung
28	chr15:58951600-58976400	Weak transcription	GM12878-XiMat	blood
29	chr15:58951600-58981800	Weak transcription	Fetal Brain Male	brain
30	chr15:58951800-58960200	Weak transcription	Fetal Heart	heart
31	chr15:58952600-58959400	Weak transcription	HSMMtube	muscle
32	chr15:58952600-58960600	Weak transcription	Fetal Intestine Small	intestine
33	chr15:58955000-58971800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr15:58955200-58971800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr15:58955200-58971800	Weak transcription	Fetal Muscle Leg	muscle
36	chr15:58955200-58971800	Weak transcription	Fetal Stomach	stomach
37	chr15:58955200-58971800	Weak transcription	Left Ventricle	heart
38	chr15:58955200-58976400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:58955200-58988400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr15:58955400-58971200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr15:58955400-58976200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr15:58955800-58970800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr15:58955800-58972000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr15:58956400-58959400	Weak transcription	Osteobl	bone
45	chr15:58956400-58960800	Weak transcription	Fetal Intestine Large	intestine
46	chr15:58956400-58967800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr15:58956600-58960000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr15:58956600-58961400	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr15:58956600-58967800	Weak transcription	Fetal Kidney	kidney
50	chr15:58956600-58974800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links